Blayau, Martine

Molecular screening ofSHH,ZIC2,SIX3, andTGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations

Dubourg, C., Lazaro, L., Pasquier, L., Bendavid, C., Blayau, M., Duff, F. L., Durou, M.-R., Odent, S., & David, V. (2004) · Human Mutation

Fetal and Pediatric Neurological DisordersHedgehog Signaling Pathway Studies

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Cystic fibrosis patients with the 3272-26A>G splicing mutation have milder disease than F508del homozygotes: a large European study

Amaral, M. D., Pacheco, P., Beck, S., Farinha, C. M., Penque, D., Nogueira, P., Barreto, C., Lopes, B., Casals, T., Dapena, J., et al. (2001) · Journal of Medical Genetics

Cystic Fibrosis Research AdvancesGenetic and Kidney Cyst Diseases

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